Senior Process Development Engineer

Senior Process Development Engineer

Canton, IL (onsite )

Contract :- 12 MONTH

Please note: All candidates must be U.S. Citizens or Green Card holders.

I'm reaching out because I need your support on a new Process Development opportunity with our client, located in Canton, IL. This is a year‑long contract role, with the possibility of extension or even conversion to direct hire.

Please note: All candidates must be U.S. Citizens or Green Card holders.

Below are the key details for the position:

Job Responsibilities:

• Lead development, validation, and implementation of manufacturing processes for new medical devices

• Collaborate closely with R&D, Operations, Quality, and Regulatory teams

• Apply principles of Design for Manufacturability, Lean, and risk‑based process development

• Drive Make vs. Buy analysis and support supplier selection

• Own key process documentation (PFMEAs, instructions, drawings, etc.)

• Contribute to successful transfer of devices from development to sustaining production

Desired Qualifications:

• Bachelor's degree in Engineering

• 5+ years' experience in Class II/III medical device manufacturing

• Strong background in process validation, ISO 13485/FDA requirements, GMP, and Lean

• Experience collaborating in multidisciplinary teams

• Excellent communication and project leadership skills

There will be two interview rounds for this role. If you have strong candidates who would be a good fit, please send them my way. I appreciate your partnership and look forward to working together on this important search.